A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5845967



Internal ID22620902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75532114..75548649hg38UCSC Ensembl
chr6:76241830..76258365hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3816536
hg1916536
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5845967
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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